Patient-reported outcomes in the evaluation of toxicity of anticancer treatments

Author:

Di Maio Massimo,Basch Ethan,Bryce Jane,Perrone Francesco

Publisher

Springer Science and Business Media LLC

Subject

Oncology

Reference43 articles.

1. U.S. Food and Drug administration. Food and Drug Administration's overall risk management activities. [online] , (2015).

2. European Medicines Agency. Reflection paper on benefit-risk assessment methods in the context of the evaluation of marketing authorisation application of medicinal products for human use. [online] , (2008).

3. European Medicines Agency. Guideline on the evaluation of anticancer products in man. [online] , (2012).

4. The National Cancer Institute. Common terminology criteria for adverse events, version 3.0. [online] , (2006).

5. U.S. Food and Drug Administration. Clinical Outcome Assessment (COA): glossary of terms. [online] , (2015).

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